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Fine-Scale Structure Analysis Shows Epidemic Patterns of Clonal Complex 95, a Cosmopolitan Escherichia coli Lineage Responsible for Extraintestinal Infection

Identifieur interne : 000C16 ( Main/Exploration ); précédent : 000C15; suivant : 000C17

Fine-Scale Structure Analysis Shows Epidemic Patterns of Clonal Complex 95, a Cosmopolitan Escherichia coli Lineage Responsible for Extraintestinal Infection

Auteurs : David M. Gordon [Australie] ; Sarah Geyik [Australie] ; Olivier Clermont [France] ; Claire L. O Rien [Australie] ; Shiwei Huang [Australie] ; Charmalie Abayasekara [Australie, Sri Lanka] ; Ashwin Rajesh [Australie] ; Karina Kennedy [Australie] ; Peter Collignon [Australie] ; Paul Pavli [Australie] ; Christophe Rodriguez [France] ; Brian D. Johnston [États-Unis] ; James R. Johnson [États-Unis] ; Jean-Winoc Decousser [France] ; Erick Denamur [France]

Source :

RBID : PMC:5451516

Abstract

Escherichia coli clonal complex 95 represents a cosmopolitan, genetically diverse lineage, and the extensive substructure observed in this lineage is epidemiologically and clinically relevant. The frequency with which CC95 strains are responsible for extraintestinal infection appears to have been stable over the past 15 years. However, the different subgroups identified within this lineage have an epidemic structure depending on the host, sample, continent, and time. Thus, the evolution and spread of strains belonging to CC95 are very different from those of another cosmopolitan human-associated clonal complex, CC131, which has increased significantly in frequency as a cause of extraintestinal infection over the past 15 years due to the evolution and spread of two very closely related, nearly monomorphic lineages.


Url:
DOI: 10.1128/mSphere.00168-17
PubMed: 28593194
PubMed Central: 5451516


Affiliations:


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Le document en format XML

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<wicri:noRegion>Australian Capital Territory</wicri:noRegion>
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</author>
<author>
<name sortKey="Pavli, Paul" sort="Pavli, Paul" uniqKey="Pavli P" first="Paul" last="Pavli">Paul Pavli</name>
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<country xml:lang="fr">Australie</country>
<wicri:regionArea>Medical School, Australian National University, Canberra, Australian Capital Territory</wicri:regionArea>
<wicri:noRegion>Australian Capital Territory</wicri:noRegion>
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<affiliation wicri:level="1">
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<country xml:lang="fr">Australie</country>
<wicri:regionArea>Gastroenterology and Hepatology Unit, Canberra Hospital, Canberra, Australian Capital Territory</wicri:regionArea>
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<author>
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<country xml:lang="fr">France</country>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>VA Medical Center and Department of Medicine, University of Minnesota, Infectious Diseases, Minneapolis, Minnesota</wicri:regionArea>
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<author>
<name sortKey="Johnson, James R" sort="Johnson, James R" uniqKey="Johnson J" first="James R." last="Johnson">James R. Johnson</name>
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<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>VA Medical Center and Department of Medicine, University of Minnesota, Infectious Diseases, Minneapolis, Minnesota</wicri:regionArea>
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<author>
<name sortKey="Decousser, Jean Winoc" sort="Decousser, Jean Winoc" uniqKey="Decousser J" first="Jean-Winoc" last="Decousser">Jean-Winoc Decousser</name>
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<country xml:lang="fr">France</country>
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<author>
<name sortKey="Denamur, Erick" sort="Denamur, Erick" uniqKey="Denamur E" first="Erick" last="Denamur">Erick Denamur</name>
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<country xml:lang="fr">France</country>
<wicri:regionArea>UMR 1137 INSERM and Université Paris Diderot, IAME, Sorbonne Paris Cité, Paris</wicri:regionArea>
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<settlement type="city">Paris</settlement>
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<affiliation wicri:level="3">
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<country xml:lang="fr">France</country>
<wicri:regionArea>Assistance Publique: Hôpitaux de Paris, Hôpital Bichat, Paris</wicri:regionArea>
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<series>
<title level="j">mSphere</title>
<idno type="eISSN">2379-5042</idno>
<imprint>
<date when="2017">2017</date>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>
<italic>Escherichia coli</italic>
clonal complex 95 represents a cosmopolitan, genetically diverse lineage, and the extensive substructure observed in this lineage is epidemiologically and clinically relevant. The frequency with which CC95 strains are responsible for extraintestinal infection appears to have been stable over the past 15 years. However, the different subgroups identified within this lineage have an epidemic structure depending on the host, sample, continent, and time. Thus, the evolution and spread of strains belonging to CC95 are very different from those of another cosmopolitan human-associated clonal complex, CC131, which has increased significantly in frequency as a cause of extraintestinal infection over the past 15 years due to the evolution and spread of two very closely related, nearly monomorphic lineages.</p>
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